1,645 Pharmaceutical Manufacturing jobs in the United States

Front Range Staffing is seeking Pharmaceutical Manufacturing Technicians with 2 years of experience in pharmaceutical or nutraceutical production. This role is ideal for someone familiar with machine operation, weighing and blending materials, and in Manufacturing Technician, Technician, Pharmaceutical, Manufacturing, Staffing

• Maintaining the pharmacy and manufacturing areas and equipment in a clean, neat and orderly manner.

• Requisitioning materials needed from warehouse. Verifying all materials received are correct, released, and within the expiry period.

• Weighing raw materials according to master records and record all dispensing information in an accurate and timely manner. Dispensing material on a first in/first out basis. Labeling all containers appropriately.

• Cleaning all areas and equipment to be used. Completing appropriate logbooks prior to requesting Quality Assurance clearance.

• Verifying that all necessary materials are correct, present, and released. Obtaining supervisory verification of all weights and measurements to assure correctness of quantities and calculations prior to processing. Assuring that all outer containers are free from dust and debris.

• Processing raw materials according to instructions, documenting all required actions in the master records. Operating all equipment in a safe manner according to established procedures.

• Performing in-process testing as required in the master instructions, and document appropriately. Monitoring the product being processed to assure compliance with all in-process specifications.

• Weighing and documenting yield for all products after completion. Labeling all product containers and reject materials appropriately.

• Transferring completed products to the proper in-process quarantine area or processing area as appropriate.

• Cleaning the manufacturing areas and equipment promptly at the conclusion of each operation. Cleaning hoses used to transfer purified water according to schedule. Sanitizing the floor drains according to schedule.

• The individual selected for this role must like working in a fast paced but highly compliant environment.
• Team player.
• Reliable, self-starting, and organized.
• Able to follow clear instructions.
• Attention to detail.
• Robust communication skills (oral and written).
• Flexible work hours.

• High School diploma or equivalent, with good mathematical skills.
• Experience in food or pharmaceutical manufacturing a plus.
• Experience in a manufacturing facility in compliance with 21CFR Part 211--cGMP is preferred
• Fluency in the English language is required.
• 1st and 2nd Shift openings
• Must be able to work overtime if required

• Must be able to life at least 65 lbs
• Must be able to perform required repetitive lifting tasks.
• Lifting, walking, repetitive hand motions and attentiveness required.
• Climb ladders and stairs, walking, bending, stooping is required.
• Occasional heavy lifting or moving required.
• The ability to gown and work successfully in a clean room environment.
• The ability to wear a respirator is required.

Be the Expert Behind Life-Changing Therapies - Join Us as a Process Expert!

Location: Onsite in Millburn, NJ | Shift: Monday-Friday, 9:00 AM - 5:30 PM

Pay Range: $35.71 - $9.29/hour

At PDS Tech Commercial , we're partnering with a leading name in Pharmaceutical Manufacturing to deliver innovation and excellence in Radioligand Therapy (RLT) . We're searching for a Process Expert who's ready to make an immediate impact-ensuring top-tier quality and compliance on the shop floor of a high-tech, purpose-driven production environment.

Make a Difference Where Precision Matters

As a Process Expert , you'll be a key player in supporting the execution of clinical and commercial batch manufacturing. You'll own deviation investigations, drive continuous process improvements, and play a central role in maintaining regulatory compliance-all while fostering a culture of collaboration and accountability.

What You'll Do:

• Lead timely and thorough investigations of process deviations, including Out of Specification (OOS) and Out of Expectation (OOE) results

• Collaborate across departments to determine root causes and assess impact

• Initiate and monitor CAPAs, ensuring implementation and effectiveness

• Serve as change manager for manufacturing change controls to support process and quality improvements

• Escalate critical issues per company procedures and clearly communicate findings and resolutions

• Draft and review GMP-compliant manufacturing documentation

What You Bring:

Required:

• Bachelor's degree (science or related discipline preferred)

• At least 1 year of GMP experience in a manufacturing setting

• Familiarity with pharmaceutical production processes

• Solid understanding of deviation and CAPA management

• Proficiency in technical writing and regulatory documentation

• Strong communication skills and the ability to work cross-functionally

Preferred:

• Experience in radiopharmaceuticals or sterile drug manufacturing

• Lean/Six Sigma or continuous improvement training/certification

Why Join Us?

At PDS Tech Commercial, you're not just another contractor-you're a valued team member. We partner with innovative companies where your work fuels meaningful change. In this role, you'll be part of a fast-paced environment where your expertise helps deliver therapies that matter . We offer competitive pay, consistent weekday hours, and the opportunity to grow your career in one of the most impactful areas of pharma manufacturing.

Join a Military Friendly® Employer committed to supporting veterans and service members

Apply Today - Build a Career That Makes a Difference

Ready to lead from the floor and make a measurable impact in the world of pharmaceutical innovation?

Apply now to become a Process Expert in Millburn, NJ!

Pay Details: $ 5.71 to 39.29 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act

• Los Angeles City Fair Chance Ordinance

• Los Angeles County Fair Chance Ordinance for Employers

• San Francisco Fair Chance Ordinance

Randstad is seeking skilled Coating Operators for a leading client in the pharmaceutical manufacturing sector. This is an excellent opportunity to work in a state-of-the-art facility with a company focused on quality, safety, and innovation.

Qualifications:

• Prior experience as a Coating Operator in a pharmaceutical or nutraceutical environment
• Knowledge of coating equipment such as Accela-Cota or similar systems
• Understanding of cGMP guidelines

Job DescriptionJob Description

Manufacturing Technician I  

THIS POSITION IS NOT ELIGIBLE FOR VISA SUPPORT OF ANY KIND, CURRENTLY OR IN THE FUTURE, AND SUCH SPONSORSHIP WILL NOT BE PROVIDED. 
 
Where science meets innovation, and YOU make the difference! 

About AustinPx 

At AustinPX, we’re not just advancing science—we’re accelerating it! We partner with the world's leading pharmaceutical companies to develop and deliver life-changing treatments to patients faster. And now, we’re on the hunt for fresh talent to help us on this mission and to develop into future pharmaceutical leaders! Ready to contribute to life-changing projects, and have a blast doing it? Then read on! 

AustinPx is a contract development and manufacturing organization (CDMO) specializing in preclinical through Phase II formulation and process development and GMP manufacturing of oral dosage forms. We specialize in bioavailability enhancement, including our next amorphous dispersion platform, KinetiSolTM Technology. At AustinPx, we recruit and develop exceptional individuals with a passion for science and determination to excel. We offer a technically challenging and stimulating environment and the opportunity to grow and advance in your career.  

AustinPx is committed to a culture of respect and excellence in everything we do.   As a customer-facing organization, we are laser focused on providing client-centric service. Serving our clients well goes beyond technical knowhow - it requires strong communication skills, a commitment to quality, integrity and respect for our colleagues and clients. We want people who are passionate about pharmaceutical development, have a sense of urgency, and enjoy solving problems. 

We offer a comprehensive suite of health and retirement benefits, resources and programs to meet your and your family’s needs. Our positive and fast-paced working environment is continually focused on improving processes to remain innovative and dynamic. 

Position Description 

The Manufacturing Technician I is responsible for production of pharmaceutical solid oral dosage forms for Phase I and II clinical trials. Under the direction of the Manufacturing Director or Supervisor, adhering to current Good Manufacturing Practices (cGMP) and following Standard Operating procedures (SOPs), the Manufacturing Technician will work hands-on in GMP production facility. Using a variety of compounding and manufacturing equipment and technologies, including blending, granulation, encapsulation, compression, and coating tools, you will: 

• Responsible for manufacturing of cGMP (Good Manufacturing Practices) products, following SOP’s (Standard Operating Procedures), and providing accurate documentation in production batch records. 

• Daily responsibilities vary and include equipment and room set up, breakdown and clean up, weighing of materials, running equipment, troubleshooting equipment, samples submission, and packaging. 

• Operates automated or semi-automated equipment. 

• Prepares materials and equipment for production. 

• Supports equipment cleaning verification and validation activities. 

• Assist with the warehouse, stocking, receiving, and shipping. 

• Other duties as assigned. 

• This is a full-time hourly position on 1st shift Monday-Friday with hours of 7:30am-4:00pm, though these hours may vary to meet the needs of the production schedule. 

What We’re Looking For: 

• High School Diploma or GED equivalent is required. Prior coursework or experience working within a regulated environment (GMP/FDA/DEA/OSHA), is highly . 

• Mechanical and technical aptitude and the desire to work in a regulated environment and strictly follow procedures is required to be successful in this position.   

• Communication Skills: Ability to read, write, and comprehend reports, technical and cGMP documents as well as correspondence. 

• There is no “i” in Team:  A team player with a positive attitude and able to take initiative. Strong attention to detail, safety, quality and client requirements is critical. Critical thinking skills with the ability to proactively point out areas for improvement or to avoid risks.  

• Physical Requirements: This position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently. 

• Cabbage: The annual pay range for this position is $40,000 – $46,000 annually. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.  Relocation Assistance is NOT available for this position. 

Why AustinPX? 

• Real Impact: Your work could play a part in getting life-saving medications to patients sooner. 

• Mentorship: Learn from experts in the field (who also happen to be pretty awesome people). 

• Work Hard, Play Hard: Enjoy fun team activities, such as corn-hole tournaments, movie day, floats on the river, and puzzles and board games.  

• Career Growth: AustinPx offers rewarding opportunities to further your career! Individuals who show promise and a commitment to growth have the opportunity to expand their career. 

• Benefits: Generous 401K match, Paid Time Off accrual, and 10+ paid holidays/year, Medical, Dental and Vision benefits.  Life Insurance, Short Term and Long Term also provided.  

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